Stereochemistry of enacyloxins. Part 6: Synthesis of C16′-C23′ fragments of enacyloxins, a series of antibiotics from Frateuria sp. W-315

Wataru Igarashi, Hiroaki Hoshikawa, Hiroyuki Furukawa, Teiko Yamada, Shigefumi Kuwahara, Hiromasa Kiyota

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

The C16′-C23′ fragments of enacyloxins, a series of antibiotics isolated from Frateuria sp. W-315, were synthesized from D-arabinose.

Original languageEnglish
Pages (from-to)7-9
Number of pages3
JournalHeterocyclic Communications
Volume17
Issue number1-2
DOIs
Publication statusPublished - Jul 2011
Externally publishedYes

Fingerprint

Stereochemistry
Arabinose
Anti-Bacterial Agents

Keywords

  • Antibiotics
  • D-arabinose
  • Enacyloxins
  • Frateuria sp. W-315
  • Synthesis
  • Wittig-Horner reaction

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Stereochemistry of enacyloxins. Part 6 : Synthesis of C16′-C23′ fragments of enacyloxins, a series of antibiotics from Frateuria sp. W-315. / Igarashi, Wataru; Hoshikawa, Hiroaki; Furukawa, Hiroyuki; Yamada, Teiko; Kuwahara, Shigefumi; Kiyota, Hiromasa.

In: Heterocyclic Communications, Vol. 17, No. 1-2, 07.2011, p. 7-9.

Research output: Contribution to journalArticle

Igarashi, Wataru ; Hoshikawa, Hiroaki ; Furukawa, Hiroyuki ; Yamada, Teiko ; Kuwahara, Shigefumi ; Kiyota, Hiromasa. / Stereochemistry of enacyloxins. Part 6 : Synthesis of C16′-C23′ fragments of enacyloxins, a series of antibiotics from Frateuria sp. W-315. In: Heterocyclic Communications. 2011 ; Vol. 17, No. 1-2. pp. 7-9.
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